The synthesis of (±)-pallescensin A

DOI: 10.1007/BF02503794

Source and publish data:

Russian Chemical Bulletin p. 1956 - 1960 (1997)

Update date:2022-08-03

Topics:

Authors:

Moiseenkov

Surkova Surkova

Lozanova

Veselovsky

Read Full Text PDF DownLoad Join now for total 90,000,000 free articles

Article abstract of DOI:10.1007/BF02503794

The racemic form of the metabolite of the Dysidea sea sponge, furanoterpenoid pallescensin A, was synthesized by cationic cyclization of the sulfonyl-substituted linear sesquiterpene precursor.

Full text of DOI:10.1007/BF02503794

Products guided by the article

Product name:(E)-4-Benzenesulfonyl-7,11-dimethyl-3-methylene-dodeca-6,10-dien-1-ol

Cas No:202803-96-1

R&D Labs maybe for 202803-96-1

Quzhou Hopemax Chemical Technology Co.Ltd

Contact:86-570-3036007

Address:Room 801,Building 2,Wealth Center,No.51,Xujiang Road,Quzhou,China.
Wuhan Pengo Technology.,Ltd.

Contact:+86-27-67841589

Address:Add: 999 Gaoxin Road, Donghu New Technology Development Zone, Wuhan City, Hubei, China
Nanjing Fayekong Chemcial Co.,Ltd(expird)

Contact:86-25-58813444

Address:Rm 1503, Unit 1, Building 5, Zijinnanyuan, Nanjing, Jiangsu, China
Wuhan Sunrise Pharmaceutical Technology Co., Ltd

Contact:+86-27-83314682

Address:Room 340, New material Industrial base No.17, Gu Tian Five Lu , Qiaokou District, Wuhan , China
Zhejiang Chemicals Import & Export Corporation

Contact:86-571-87043088

Address:No.37,Qingchun Road,Hangzhou,China

Relevant to this article

Preparation, Ligand Substitution, and Structural Stability of (eta;³-Allyl)dicarbonylnitrosyliron Complexes

Doi:10.1246/bcsj.71.403
(1998)
Neomycin-capped aromatic platforms: Quadruplex DNA recognition and telomerase inhibition

Doi:10.1039/b516378a
(2006)
Diels-Alder cycloaddition of electrophilic 2H-azirines with 3-(3-(tert-butyldimethylsilyloxy)buta-1,3-dienyl)oxazolidin-2-ones. Treatment of the cycloadducts under acidic conditions

Doi:10.1016/j.tet.2006.01.035
(2006)
Optimization of a potent class of arylamide colony-stimulating factor-1 receptor inhibitors leading to anti-inflammatory clinical candidate 4-cyano-N -[2-(1-cyclohexen-1-yl)-4-[1-[(dimethylamino)acetyl]-4-piperidinyl]phenyl]-1 H -imidazole-2-carboxamide (JNJ-28312141)

Doi:10.1021/jm200900q
(2011)
SYNTHESIS OF CELLOBIOSE, CELLOTRIOSE, CELLOTETRAOSE, AND LACTOSE

Doi:10.1016/0008-6215(83)84014-2
(1983)
Synthesis and structure-activity relationships of naphthamides as dopamine D₃ receptor ligands

Doi:10.1021/jm0100077
(2001)

Article Doi